Canonical Allele Identifier: CA1021917108
Gene: OLIG2 HGNC NCBI

Linked Data

dbSNP Id: rs1981064843
gnomAD v3: 21-33026170-T-C
gnomAD v4: 21-33026170-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33026170T>C , CM000683.2:g.33026170T>C GRCh38
NC_000021.8:g.34398478T>C , CM000683.1:g.34398478T>C GRCh37
NC_000021.7:g.33320348T>C NCBI36
NG_011834.1:g.5240T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382357.4:c.-63+144T>C MANE Select ENSP00000371794.3:n.-63+144T>C
ENST00000333337.3:c.-693T>C ENSP00000331040.3:n.-693T>C
ENST00000382357.3:c.-63+144T>C ENSP00000371794.3:n.-63+144T>C
ENST00000430860.1:c.-153T>C ENSP00000391183.1:n.-153T>C
NM_005806.3:c.-63+144T>C NP_005797.1:n.-63+144T>C
XM_005260908.1:c.-153T>C XP_005260965.1:n.-153T>C
NM_005806.4:c.-63+144T>C MANE Select NP_005797.1:n.-63+144T>C
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